Primary Site >> Stomach Cancer
Gene >> LARP6
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000299213 |
| Start | 70832101:70832101(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1427A>C |
| AA Mutation | p.Asp476Ala(p.D476A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000299213 |
| Start | 70832602:70832602(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs368859399 |
| CDS Mutation | c.926A>G |
| AA Mutation | p.Glu309Gly(p.E309G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000299213 |
| Start | 70832183:70832183(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1345G>A |
| AA Mutation | p.Gly449Ser(p.G449S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000299213 |
| Start | 70832607:70832607(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs760442315 |
| CDS Mutation | c.921C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000299213 |
| Start | 70836442:70836442(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs150115251 |
| CDS Mutation | c.264G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000299213 |
| Start | 70832989:70832989(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.539delA |
| AA Mutation | p.Asn180ThrfsTer34(p.N180Tfs*34) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |